在时间依赖密度函数理论中,长距离校正交换-相关函数的稳定性和代理程序函数的稳定性
Jared R Williams1, Carsten A Ullrich1
1Department of Physics and Astronomy, University of Missouri, Columbia, Missouri 65211, United States.
Journal of chemical theory and computation
|April 24, 2025
概括
取决于时间的长距离校正 (LRC) 函数能改善激电动力学模拟,但可能导致不稳定性. 一种新的稳定方法通过纠正违反零力定理的情况来解决这些问题.
科学领域:
- 计算物理 计算物理
- 量子化学 是一个量子化学.
- 材料科学 材料科学 材料科学
背景情况:
- 固体中的刺激效应对于光学吸收光谱至关重要.
- 时间依赖密度功能理论 (TDDFT) 描述了这些效应.
- 长距离校正 (LRC) 函数已扩展到实时TDDFT,用于刺激子动态.
研究的目的:
- 为了研究时间依赖的LRC方法的数值稳定性.
- 了解基于LRC的激子动态模拟中的不稳定性的起源.
- 为时间依赖的LRC方法开发一个强大的数值稳定方案.
主要方法:
- 用一个二维模型固体进行数值模拟.
- 利用时间依赖的Kohn-Sham方程与一个LRC矢量潜力.
- 分析了刺激子结合能和数值稳定性之间的联系.
主要成果:
- 时间依赖的LRC方法中的不稳定性随着激发的结合能增加.
- 这些不稳定性源于时间平均违反零力定理.
- 成功开发了一个简单而强大的数值稳定方案.
结论:
- 该研究确定了时间依赖的LRC TDDFT数值不稳定的根本原因.
- 提出并证明了一种新的稳定方法,提高了模拟的可靠性.
- 这项工作验证并解释了Proca程序函数用于稳定LRC矢量潜力的有效性.
更多相关视频
13:56Probe Type II Band Alignment in One-Dimensional Van Der Waals Heterostructures Using First-Principles Calculations
Published on: October 12, 2019
7.5K
08:04Excitonic Hamiltonians for Calculating Optical Absorption Spectra and Optoelectronic Properties of Molecular Aggregates and Solids
Published on: May 27, 2020
8.3K
相关概念视频
Stability of Equilibrium Configuration
414
Understanding the stability of equilibrium configurations is a fundamental part of mechanical engineering. In any system, there are three distinct types of equilibrium: stable, neutral, and unstable.
A stable equilibrium occurs when a system tends to return to its original position when given a small displacement, and the potential energy is at its minimum. An example of a stable equilibrium is when a cantilever beam is fixed at one end and a weight is attached to the other end. If the weight...
A stable equilibrium occurs when a system tends to return to its original position when given a small displacement, and the potential energy is at its minimum. An example of a stable equilibrium is when a cantilever beam is fixed at one end and a weight is attached to the other end. If the weight...
414
MO Theory and Covalent Bonding
10.2K
The molecular orbital theory describes the distribution of electrons in molecules in a manner similar to the distribution of electrons in atomic orbitals. The region of space in which a valence electron in a molecule is likely to be found is called a molecular orbital. Mathematically, the linear combination of atomic orbitals (LCAO) generates molecular orbitals. Combinations of in-phase atomic orbital wave functions result in regions with a high probability of electron density, while...
10.2K
Van der Waals Equation
3.6K
The ideal gas law is an approximation that works well at high temperatures and low pressures. The van der Waals equation of state (named after the Dutch physicist Johannes van der Waals, 1837−1923) improves it by considering two factors.
First, the attractive forces between molecules, which are stronger at higher densities and reduce the pressure, are considered by adding to the pressure a term equal to the square of the molar density multiplied by a positive coefficient a. Second, the...
First, the attractive forces between molecules, which are stronger at higher densities and reduce the pressure, are considered by adding to the pressure a term equal to the square of the molar density multiplied by a positive coefficient a. Second, the...
3.6K
Molecular Orbital Theory II
18.6K
Molecular Orbital Energy Diagrams
18.6K
Molecular Orbital Theory I
31.2K
Overview of Molecular Orbital Theory
31.2K
Stability of Conjugated Dienes
3.2K
Introduction
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
3.2K
